The Tramadol Metabolite O-Desmethyl Tramadol Inhibits Substance P-Receptor Functions Expressed in Xenopus Oocytes
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- Minami Kouichiro
- Department of Anesthesiology and Critical Care Medicine, Jichi Medical University, Japan Division of Cancer Pathophysiology, National Cancer Center Research Institute, Japan
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- Yokoyama Toru
- Department of Anesthesiology and Critical Care Medicine, Jichi Medical University, Japan Division of Cancer Pathophysiology, National Cancer Center Research Institute, Japan
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- Ogata Junichi
- Department of Anesthesiology and Critical Care Medicine, Jichi Medical University, Japan
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- Uezono Yasuhito
- Division of Cancer Pathophysiology, National Cancer Center Research Institute, Japan
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Tramadol has been widely used as analgesic. O-Desmethyl tramadol (ODT) is one of the main metabolites of tramadol, having much greater analgesic potency than tramadol itself. Substance P receptors (SPR) are well known to modulate nociceptive transmission within the spinal cord. In this study, we investigated the effects of ODT on SPR expressed in Xenopus oocytes by examining SP-induced Ca2+-activated Cl− currents. ODT inhibited the SPR-induced Cl− currents at pharmacologically relevant concentrations. The protein kinase C (PKC) inhibitor bisindolylmaleimide I did not abolish the inhibitory effects of ODT on SP-induced Ca2+-activated Cl− currents. The results suggest that the tramadol metabolite ODT inhibits the SPR functions, which may be independent of activation of PKC-mediated pathways.
収録刊行物
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- Journal of Pharmacological Sciences
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Journal of Pharmacological Sciences 115 (3), 421-424, 2011
公益社団法人 日本薬理学会
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詳細情報 詳細情報について
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- CRID
- 1390001205178024448
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- NII論文ID
- 10029892983
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- NII書誌ID
- AA11806667
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- ISSN
- 13478648
- 13478613
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- NDL書誌ID
- 11010103
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- NDL
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